临床数据程序员招聘_领星生物科技（上海）有限公司最新招聘信息-猎才医药网

职位描述

POSITION SUMMARYWe are dedicated to transforming the way in which patients with cancer are diagnosed and treated. At GenomiCare you will work with everyone fighting the disease—patients and their families, scientists, physicians, drug developers—to raise awareness about the ongoing evolution in cancer care and to ensure we are delivering the analytic tools and molecular information required to bring the promise of personalized cancer care into routine clinical practice. As a member of our Medical Affairs department, you will be responsible for distilling the latest advances in genomic science, oncology, technology and clinical data into innovative, best-in-class clinical tools and products that will enable oncologists to determine the best treatment throughout each patient's journey with cancer.Clinical Programmers work to implement analyses as specified in statistical analysis plans, table shells, and programming requirement documents. They are responsible for extracting data from databases to produce tables, graphs, analyses, and data listings based on clinical data, for clinical data analysis or for marketing support. They may also provide input and review for the activities of other statistics and clinical programming personnel, e.g. the review of Case Report Forms, statistical analysis plans, table shells, programming requirement documents, and databases in the future. Clinical programmers work primarily in the SAS programming language, and follow standardized quality control procedures for the development, testing (including peer review), and implementation of their programs.KEY RESULT AREAS1.Perform activities and provide technical expertise in support of reporting data.2.Design and plan statistical algorithms and code in conformance with company system and demands and programming standards.3.Be accountable for implementation of statistical analyses, programmed outputs, and tables listings and graphs for integrated scientific reports for clinical trial results and support for publication activities, for assigned projects.4.Provide input into the design and development of project plans; in providing planning, development and delivery of analyses, (tables, listings and graphs), for use in scientific reports, clinical trial results, publications, regulatory response and commercialization.5.Implement strategies, initiatives, processes, and standards to ensure speed and quality of fully integrated data analyses.6.Ensure clear and timely communication with colleagues to enable improvements to be implemented during the study and also7.Liaise regularly with manager or other business owner to assess workload and priority activities and status of assigned tasks and projects.8.Provide regular feedback as to the efficiency and effectiveness of current procedures/jobs to manager.9.Work with other line functions e.g. bioinformatics, medical to come up with initiatives for new business or optimization of current processes.ESSENTIAL REQUIREMENTSEducation1.At least bachelor degree or equivalent in statistics, computer science, or a mathematical science2.Master's Degree preferredExperience1.1+ years relevant experience with SAS or equivalent software programming in pharmaceutical or biotech industry2.Extensive knowledge of computer systems, operating systems and analysis and reporting environments used in pharmaceutical or biotech industry. Key Competencies1.Strong understanding of the current technologies and global Analysis and Reporting environments to utilize them for efficient delivery of programming outputs.2.Expertise in the SAS programming language.3.Basic knowledge to use Windows OS, MS-Word, MS-Excel, E-Mail (MS-Outlook).4.Ability to write clear, well documented, and standardized computer programs.5.A readiness and ability to work to pre-defined programming standards.6.Strong analytical skills.7.Able to work on multiple projects simultaneously.8.Demonstrated platform skills. Experience in presenting to science and non-science audiences.9.Must be accurate and have an excellent attention to detail and a quality control approach to work.10.Utilizes and shares innovative approaches to build and maintain a competitive advantage11.Looks for opportunities for collaboration and acts upon them12.Respectfully challenges practices, decisions or ideas to uphold integrity and ethical standards.13.Contributes to a learning organization, encouraging experimentation, risk-taking, and development in all aspects of work performance. 职能类别：临床数据分析员

公司信息

领星生物是由中美生物医学科学家携手资深肿瘤专家共同开创的肿瘤精准医疗服务平台，是一家集精准医疗方案筛选、实施和监测于一体的国际化公司。公司总部位于上海，同时在美国波士顿和中国香港设有业务机构。秉承“临床价值”、“关怀”和“效率”的企业使命，领星整合了高通量测序、基因组学、医疗信息学、临床病程管理等前沿技术手段，建立起一流的医疗资源合作网络，致力于通过具有开创性的业务模式为中国肿瘤患者和医生提供个体化精准医疗的临床解决方案和面向全球资源的对接服务。在公司日常运营过程中，领星提倡以“价值”、“简单”、“快乐”为核心的企业文化。公司管理团队具有丰富的国际视野和对本土市场的深刻洞察，高度重视文化的打造和人才的培养。领星倡导在简单清晰的企业架构下，凝聚起一批具有相似价值观的员工，共同践行企业使命，实现员工和企业的同步成长。领星生物属于综合医疗服务集团嘉信控股（Carebridge Holdings），集团旗下还拥有上海嘉会国际医院和嘉会诊所等医疗机构，及负责《新英格兰医学杂志》（The New England Journal of Medicine）官方认证中文版运营的嘉会医学研究和教育集团有限公司。

周边城市招聘：上海浙江安徽广东山东河北重庆北京江苏湖南

企业入驻日期： 2017-11-09

上海相关职位

职位描述

联系方式

公司信息